Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.


  1. Advanced Patent Search
Publication numberUS9228132 B2
Publication typeGrant
Application numberUS 13/774,320
Publication date5 Jan 2016
Filing date22 Feb 2013
Priority date10 Nov 2004
Also published asCA2587205A1, EP1799796A2, EP1799796A4, US7909895, US8409303, US20060096163, US20110192074, US20130160683, USRE45869, WO2006053020A2, WO2006053020A3
Publication number13774320, 774320, US 9228132 B2, US 9228132B2, US-B2-9228132, US9228132 B2, US9228132B2
InventorsNorman L. Dickinson, Kevin M. Bolin, Brian Dooley
Original AssigneeSGC Advisors, LLC
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Slurry dewatering and conversion of biosolids to a renewable fuel
US 9228132 B2
In the processes for treating municipal sewage and storm water containing biosolids to discharge standards, biosolids, even after dewatering, contain typically about 80% water bound in the dead cells of the biosolids, which gives biosolids a negative heating value. It can be incinerated only at the expense of purchased fuel. Biosolids are heated to a temperature at which their cell structure is destroyed and, preferably, at which carbon dioxide is split off to lower the oxygen content of the biosolids. The resulting char is not hydrophilic, and it can be efficiently dewatered and/or dried and is a viable renewable fuel. This renewable fuel can be supplemented by also charging conventional biomass (yard and crop waste, etc.) in the same or in parallel facilities. Similarly, non-renewable hydrophilic fuels can be so processed in conjunction with the processing of biosolids to further augment the energy supply.
Previous page
Next page
What is claimed is:
1. A process of converting biomass into a renewable fuel comprising the steps of:
providing biomass comprising at least about 10% water;
applying sufficient pressure to the biomass to maintain liquidity and form pressurized biomass;
heating the pressurized biomass to a first temperature, wherein the first temperature is sufficient to form an aqueous biomass char slurry, carbon dioxide, and free water;
depressurizing the biomass char slurry;
separating the carbon dioxide from the biomass char slurry;
removing at least a portion of the free water from the biomass char slurry to provide a dewatered biomass char product containing a decreased oxygen content; and
utilizing the dewatered biomass char product as a fertilizer.
2. The process of claim 1, wherein the biomass comprises sewage sludge.
3. The process of claim 1, wherein the first temperature is between about 200° C. and 345° C. (400° F. and 650° F.).
4. The process of claim 1, further comprising the step of adding an agent for dissolution of at least one polluting or slag-forming element present in the dewatered biomass char product.
5. The process of claim 4, wherein the agent comprises an alkali.
6. The process of claim 1, wherein a portion of the freed water is recycled to the adding step.
7. The process of claim 1, further comprising the step of cooling the aqueous biomass char slurry to a second temperature less than the first temperature.
8. The process of claim 1, wherein the second temperature is about 40° C. to 90° C. (100° F. to 200° F.).
9. The process of claim 1, further comprising the step of discharging the carbon dioxide through a flame of at least one of an oxidizer and a process heater.
10. The process of claim 1, further comprising the step of slurrying the biomass by performing at least one of the steps of grinding and adding at least one of fresh water, recycled water, steam, process water from an adjacent wastewater treatment plant and a combination thereof to form a pumpable slurry.
11. The process of claim 1, further comprising the step of pretreating at least a portion of the free water to form pretreated water and recycling the pretreated water to an adjacent wastewater treatment plant.
12. The process of claim 1, further comprising the step of using a digester gas from an adjacent wastewater treatment plant as fuel for the heating step.
13. The process of claim 1, wherein the removing step comprises mechanically dewatering the biomass char slurry to about 35% to 65% solids for use as the fertilizer.
14. The process of claim 1, wherein the dewatered biomass char product that is used as the fertilizer is undried.
15. The process of claim 1, further comprising the step of subjecting the freed water from the removing step to digestion.
16. The process of claim 1, wherein the biomass comprises about 3% to 40% solids.
17. The process of claim 16, wherein the biomass comprises about 20% solids.
18. A process of converting biomass into a renewable fuel comprising the steps of:
providing biomass comprising at least about 10% water;
applying sufficient pressure to the biomass to maintain liquidity and form pressurized biomass;
heating the pressurized biomass to a first temperature, wherein the first temperature is sufficient to form an aqueous biomass char slurry, carbon dioxide, and free water;
depressurizing the biomass char slurry;
separating the carbon dioxide from the biomass char slurry;
removing at least a portion of the free water from the biomass char slurry to provide a dewatered biomass char product containing a decreased oxygen content; and
directing the dewatered biomass char product to a landfill.
19. The process of claim 18, wherein the removing step comprises mechanically dewatering the biomass char slurry to about 35% to 65% solids for use at the landfill.
20. The process of claim 18, wherein the dewatered biomass char product that is directed to the landfill is undried.

This application is a continuation of U.S. patent application Ser. No. 13/025,544, now U.S. Pat. No. 8,409,303, filed Feb. 11, 2011, which is a continuation of U.S. patent application Ser. No. 11/269,499, now U.S. Pat. No. 7,909,895, filed Nov. 7, 2005, which claims priority to U.S. Provisional Patent Application Ser. No. 60/626,680, filed Nov. 10, 2004, the disclosures of which are hereby expressly incorporated by reference herein in their entirety.


Sludge from sewage and wastewater treatment plants, and the biosolids it contains, represents a serious disposal problem. The Water Environment Federation (WEF) formally recognized the term “biosolids” in 1991, and it is now in common use throughout the world. The WEF defines “biosolids” as the soil-like residue of materials removed from sewage during the wastewater treatment process. During treatment, bacteria and other tiny organisms break sewage down into simpler and more stable forms of organic matter. The organic matter, combined with bacterial cell masses, settles out to form biosolids. According to USEPA, biosolids that meet treatment and pollutant content criteria “can be safely recycled and applied as fertilizer to sustainably improve and maintain productive soils and stimulate plant growth”.

The sludge is a mixture of biosolids (comprised primarily of dead organic cells which are a by-product of treating sewage and wastewater so that it can be released into open waters) and varying amounts of free water. Free water can be at least partially removed by mechanical dewatering methods. In addition to the free water, the biosolids contain cell-bound water, which can make up as much as 80% of the volume of biosolids and is impossible to remove by mechanical dewatering methods. The large amounts of water contained in such sludge give it a highly negative heat value which makes the cost of incinerating it prohibitive because large amounts of costly fuel would be required to drive off the cell-bound water. In view thereof, such sludge is presently used as landfill or as a fertilizer that can be spread over land, because sewage sludge frequently contains nitrogen and phosphor, for example. However, the sludge also contains harmful substances, generates undesirable odors, and can lead to serious contamination of the soil or the landfill from, amongst others, heavy metals.

In the processes for treating municipal sewage and storm water to discharge standards, solid constituents are concentrated into a by-product, often referred to as sewage sludge. Sewage sludge is a mass or agglomeration of dead organic cells and other solids, called biosolids, which are mixed with varying amounts of water of correspondingly varying viscosity. Irrespective of the degree to which the mass of biosolids is mechanically dewatered, the remaining mass of biosolids typically contains about 80% water, because much of the water is bound inside the dead cells, giving the biosolids mass a negative heating value, thereby making biosolids effectively useless for purposes of extracting heat value from them. Thus, biosolids still are disposed of in landfills or by spreading them on agricultural land as a fertilizer that supplies nitrogen and phosphorus. However, biosolids also may contain live viruses and pathogens and toxic heavy metals, inspiring heated opposition from environmental interests, while their high water content drastically increases the cost of transporting them to a point of use.

According to the present invention, the raw biosolids are heated following their discharge from the sewage treatment plant to rupture the cells, thereby releasing the large quantities of cell-bound water. The temperature is sufficiently high so that the cell structure is destroyed and carbon dioxide is split off to lower the oxygen content of the biosolids. This results in the formation of char that is not hydrophilic and can be efficiently dewatered and/or dried. This char is a viable renewable fuel.

In a further development of the present invention, it is possible to increase the availability of renewable fuels by converting biomass (such as untreated yard and crop waste, etc.) in the same or parallel facilities. Similarly, non-renewable hydrophilic fuels can be so processed to further augment the energy that can be extracted from biosolids in accordance with the invention.


There is a growing wave of public support for renewable energy popularly called “Green Power”. Several well-known companies, according to Power magazine for May 2003, including General Motors, IBM, Dow Chemical and Johnson & Johnson, have announced plans to purchase a portion of their power requirement from “green” sources. Some companies have even announced intentions to replace all of the electricity used in their manufacturing with “green power”. Pillars of fossil energy supply, such as Chevron, British Petroleum (BP) and Shell Oil, have announced their intentions to support environmental causes. In fact, BP is an important supplier of solar energy panels. There is a “Green Power Market Development Group” of the World Resources Institute (WRI), aiming to develop 1,000 Megawatts (MW) of new, cost-competitive “green power” by 2010.

In addition, more than a dozen state legislatures require power marketers to phase in specific and increasing percentages of power from renewable sources. New York has mandated that state agencies must buy 25% of their power from renewable sources by 2013; currently 19.3% of the energy produced in New York is generated from renewable sources (New York Public Service Commission). California has passed legislation requiring that 20% of utilities' electricity in the state be produced from renewable sources by 2017. In fact, one California utility, Pacific Gas and Electricity (PG&E), advertises that more than 30% of its electricity now comes from renewable sources. At least 36 U.S. power retailers now offer a “green power” alternative. Europe also takes renewable energy seriously, targeting 20% of its generation from renewables by 2020.

Conventional renewable energy generally covers origination from solar, wind, hydro-electric, geothermal, biomass and landfill gas. There is some question as to how the demand for renewable energy will be met. Solar and wind are growing, but from a very small base. Hydro-electric and geothermal have limited new sites and face ecological opposition. Landfill gas is limited and also criticized for air pollution. There are currently no other renewable sources which might be tapped to fill the large gap between supply and demand.

Biomass has long been used as a renewable energy source. For example, wood and forestry, as well as agricultural, by-products have been used as fuels for centuries by mechanically firing them in furnaces and boilers with high excess air and low efficiency. The National Renewable Energy Laboratory (NREL) defines biomass as: “organic matter available on a renewable basis. Biomass includes forest and mill residues, agricultural crops and wastes, wood and wood wastes, animal wastes, livestock operation residues, aquatic plants, fast growing trees and plants and municipal and industrial wastes.” According to The Sandia National Laboratory's Combustion Research Facility (CRF), combustion is involved in 85% of the world's energy use. If biomass is to make a meaningful contribution to renewable energy, it will be, directly or indirectly, as a fuel.

Sewage sludge, and the large amounts of biosolids it contains, with their cell-bound water, has not previously been considered an energy source. Due to their large bound water content, biosolids have a negative fuel value and cannot be incinerated unless heated with expensive fuel that must be purchased. Such an incineration of biosolids may be desirable to avoid having to spread them on land, thereby eliminating or at least reducing possible environmental contamination, but at a very substantial cost, namely the additional heat that must come from the fuels to incinerate them.

The production of biosolids in the U.S. is estimated to be between 7.1 and 7.6 million (short) dry tons per year. Ocean dumping has been prohibited since the 1980s. The predominant disposition is spreading the biosolids on agricultural land as a fertilizer. Other dispositions are dumping in landfills and incineration.

In 1998, the production of biosolids in Europe was reported to be 7.2 million dry metric tons, and 25% was disposed to landfills. Production is expected to increase to at least 9.4 million metric tons in 2005, land application accounting for 54%, landfilling decreasing to 19%, and incineration growing to 24%—although incineration is estimated to cost five times as much as landfilling.

In 2001, biosolids production in Japan was reported to be 1.7 million dry metric tons. 40% was composted and the remainder was incinerated or used to produce cement.

After strenuous mechanical dewatering and digestion in sewage treatment plants, the solids concentration in biosolids still only ranges from about 14-30%, and is typically no more than about 20%, which means that every ton of biosolids, treated and dewatered in accordance with the prior art, is accompanied by about four tons of water, the bulk of which is bound in the dead cells. The cost of shipping the inert water limits the distance it can be moved from its source, usually a wastewater treatment plant (WWTP). These factors give biosolids a negative value. As a result, the WWTP must pay to have someone dispose of the biosolids. Such a payment is often called a “tipping fee”.

As the options for biosolids disposal become more challenging and the disposal options are moved farther from the source, disposal costs and transportation costs have become increasingly significant economic burdens. To reduce this burden, industry has focused on volume and weight reduction. The wastewater industry has made extensive efforts to remove the water from the biosolids generated at treatment plants. A typical WWTP may employ centrifuges, belt presses, rotary presses or other processes to physically force the water from the biosolids. A polymer and other chemicals may be added to assist in dewatering. Nevertheless, such mechanical dewatering methods used by WWTPs are inefficient and costly and incapable of appreciably reducing the amount of water bound in the cells of the biosolids.

The U.S. Environmental Protection Agency (EPA) grades biosolids according to regulation “40 CFR Part 503” as Class A and Class B. This regulation concerns primarily the application of biosolids to agricultural land, to which there is vocal and growing environmental opposition. For example, environmentalists condemn the use of biosolids as a fertilizer because of their content of living disease-causing organisms (pathogens and viruses) and heavy metals (such as lead, mercury, cadmium, zinc and nickel), as well as their damage to groundwater quality. In addition, environmentalists raise concerns about “quality of life” issues, such as insects and odors, associated with biosolids. As such, land application of Class B biosolids is banned in a number of counties, and more counties and states are expected to follow. In one case, where 70% of the biosolids were Class B, the banning of land application in adjacent counties nearly doubled the tipping fee from about $125 per dry ton to about $210-$235.

Furthermore, the high cell-bound water content of biosolids makes their incineration difficult for many industries. For example, the cement industry is reputed to be the world's third largest energy user. It requires the equivalent of about 470 pounds of coal to make each ton of cement. To conserve fossil fuel, 15 cement plants in the U.S. burn fuel-quality hazardous waste, and about 35 other plants use scrap tires to supplement fossil fuel. A growing method of disposing of biosolids is to incinerate them in cement kilns. Since their net fuel value is negative, this practice is only viable because of the revenue received by the kiln operator, for example, from the tipping fee, since additional fuel, such as coal, must be fired to eliminate the water bound in biosolids. In addition, in the manufacture of cement, certain elements contained in biosolids, such as chlorine, phosphorus, sodium and potassium, are not desired because they adversely affect the quality of the cement.

In the past, the requirement to dispose of biomass in general was coupled with attempts to extract heat energy from it in order to reduce disposal costs and the environmental burden of landfills. Attempts to extract energy from such materials were limited to combusting low-grade fuels and solid waste. For example, previous processes for deriving fuel from municipal solid waste (MSW) generally focus on adding alkali to assist in the removal of the majority of contained chlorine in the form of PVC found in MSW. In addition, various methods for processing relatively low-grade carbonaceous fuel, such as sub-bituminous and lignite coals, are known to those of ordinary skill in the art. In both scenarios, however, low-grade fuels are used as raw materials.

A number of schemes for the pyrolysis of biosolids have been advanced. However, they all have been forced to contend with the fact that biosolids contain about four times as much water as solid material, even after conventional dewatering at the treatment plant, for example. It is impossible to reach pyrolysis temperatures until all of the water has been vaporized, which requires at least 4000 Btu per pound of solids, which, at best, might be equal to its fuel value, before allowing for capital and operating costs.

As the foregoing demonstrates, the disposal of biosolids has become increasingly expensive and controversial. A need exists in the art for a method to cleanly and economically dispose of biosolids. The current invention provides a method to dispose of biosolids while concurrently producing an economically more viable renewable fuel.

To the extent that biosolids alone cannot meet the growing demand for renewable energy, the biosolids conversion to a useable fuel in according with the present invention can be combined with extracting energy from other sources such as biomass. Thus, the present invention provides a method and system to convert biosolids, alone or with biomass, into a viable renewable fuel in an environmentally benign manner.


As understood by applicants, biosolids are composed primarily of dead cells which have cell-bound water. When subjected to sufficient pressure to keep the water liquid, a heating of a slurry or sludge containing biosolids to a first, relatively lower, temperature causes the biosolids cells to rupture, which liberates the water bound inside the cells and thereby converts the biosolids from a substance which cannot practically be dewatered to a new fuel from which the water can be readily removed mechanically. The further heating of the biosolids additionally splits off carbon dioxide, thereby lowering the oxygen content of the biosolids and converting the biosolids into char. Once dewatered, the char has a positive heating value and can be used directly as a fuel, thereby releasing the heat energy that was previously inaccessibly bound in the biosolids.

For example, in combination with a wastewater treatment plant (WWTP), the present invention provides a method to produce a viable, renewable fuel from biosolids by converting the biosolids into a relatively dry, combustible material. In many cases, the process can be integrated with the existing infrastructure of the WWTP. Since the treated biosolids have substantially no bound water, freed water from the cells can be returned to the WWTP. The remaining cell materials become much less hydrophilic, which gives them a positive heating value and allows them to be shipped to the desired destination at a much reduced cost. If the WWTP is equipped with an anaerobic digestion stage, the gas produced can support the fluid deoxidation with fuel used in its operation. Pathogens are destroyed, and when the dewatered biosolids are heated sufficiently to carbonize them, the resulting char product contains reduced levels of most water-soluble impurities, including sodium, potassium, sulfur, nitrogen, chlorine and organic compounds, which are separated with the excess water. Biosolids char is a new player on the energy scene and is a low-cost, renewable fuel for many energy-consuming industries.

Although acceptable to incinerators and landfills, biosolids char is most productively used where its energy content is utilized. For example, in one embodiment, the method and system of the present invention is used in conjunction with a cement kiln to increase the thermal efficiency of the cement kiln and cement manufacture, while disposing of biosolids that would otherwise constitute undesirable waste. In addition, the inert material found in the biosolids can become a part of the product. Therefore, not only is the heating value in biosolids utilized, but the inerts leave no negative by-products from this configuration.

Since biosolids are produced as a viscous slurry, little preparation is required, except blending for uniformity. Following heating of the biosolids slurry under pressure to a temperature at which the cell walls rupture, the further heating of the biosolids results in a significant molecular rearrangement of the cells, splitting off of a substantial proportion of its oxygen as carbon dioxide, which carbonizes organic substances and yields so-called char that is readily incinerated. The temperature necessary for this molecular rearrangement varies but is typically between 177° C. and 315° C. (350° F. and 600° F.). The aggressively hydrolyzing conditions free anions to dissolve in the aqueous phase. Previously bound cations, such as sodium and potassium, are likewise made accessible to aqueous dissolution and subsequent removal and/or disposal.

Compared to the incineration of (raw) biosolids, in cement kilns or dedicated incinerators, the positive energy content of biosolids char substantially decreases the amount of supplemental fuel which must be purchased. Moreover, soluble cations, sources of low temperature slag in boilers and undesirable in cement, have been largely removed with the freed water.

Cement kiln and incinerator facilities may prefer for the char to be dewatered to a maximum extent, resulting in the delivery and charging of a wet solid “char” containing only about 40% to 50% water, which is about one-fifteenth of that found in the raw biosolids. Alternatively, transport and handling considerations may cause such facilities to prefer char which has been dried and compacted or pelletized. The present invention has the capability to deliver char in either form.

In addition, the biosolids char produced with this invention, with or without char from other substances such as biomass, for example, provides a fuel that is useful to a variety of other fuel-consuming industries, including blast furnaces, foundries, utility boilers, the power industry, the paper industry, and other fossil fuel-utilizing industries. For example, the present invention contemplates a green power station where biosolids char is charged to a pulverized fuel or fluidized bed combustor to generate steam, or to a gasifier feeding clean fuel gas to an integrated gas-fired gas turbine combined cycle.

Furthermore, the char produced by the present invention can be the raw material for hydrogen fuel cells through partial oxidation to a fuel gas (largely carbon monoxide and hydrogen), followed by the water gas shift and the separation of carbon dioxide, as practiced in synthetic ammonia technology. It can be “refined” into liquid fuels by adaptations of “catalytic cracking”, “delayed coking” and “hydrocracking”, patterned after the established processes well known to the petroleum refining industry.

While the present invention is directed to the economic and ecologically sound disposition of biosolids, it can be combined with appropriately treated other substances, primarily biomass that requires disposal, including, but not limited to, paper mill sludge, food waste, agricultural wastes, hog manure, chicken litter, cow manure, rice hulls, bagasse, green waste, municipal solid waste, medical waste, paper waste, wood and wood waste, palm oil residue, refuse derived fuels, Kraft Mill black liquor, and short rotation energy crops, as well as hydrophilic non-renewable fuels such as low-rank coals.

In particular, the present invention relates to a process of converting biosolids into an economically viable fuel by applying sufficient pressure to the biosolids to maintain liquidity, heating the pressurized biosolids to a sufficient temperature to rupture cells and then to evolve carbon dioxide, depressurizing the resulting char slurry, separating the carbon dioxide from the char slurry, and removing at least a portion of the aqueous phase from the char slurry to provide an at least partially dewatered char product for further use. Additionally, the invention relates to reacting the dewatered char product with a gas comprising oxygen to thereby convert its fuel value into thermal energy and using the thermal energy or incinerating the fuel.

In sum, the present invention provides an environmentally acceptable disposition of biosolids, as well as energy for various energy consumers, such as cement kilns and electric power plants. In addition, the present invention provides: (a) a method to increase the availability and environmental acceptability of renewable fuels; (b) a method to minimize the quantity of wastes to be landfilled; (c) a process to reduce the moisture (water) content of waste going to landfill; (d) a process to raise the softening point of renewable fuel ash to reduce fouling and slagging; (e) a method of converting a non-uniform solid fuel, such as agricultural and forestry waste and/or paper mill sludge, into a uniform fuel; (f) a method to convert a bulky fuel into a fuel that is compact and easy to store and transport; (g) a process to convert a perishable fuel into a sterile fuel that is storable without deterioration; (h) a method to provide an economical means of co-firing an otherwise non-compliant fuel; (i) a method to provide a thermally efficient combination of liquid deoxidation and at least one of a wastewater treatment plant, a cement kiln, and a thermal power station; (j) a method to dry biosolids prior to introduction to a cement kiln or other similar facility; (k) a method to reduce the amount of water introduced to a cement kiln and other combustors; (l) a process to co-process multiple feedstocks utilizing fluid deoxidation; (m) a method to utilize the ash in biosolids and other biomass; (n) a method to remove (and recover) elements found in biosolids or other biomass such as phosphorus, chlorine or CO2; and (o) a process to remove the water from biosolids and biomass in order to further refine these materials or to reduce disposal costs or to utilize for fertilizer.

Thus, the present invention provides a method for the disposal of sludge generated at sewage and wastewater treatment plants in an economical and environmentally benign manner. The method is economically benign because the end product is ash that is free of odors, as well as harmful substances such as viruses or pathogens, and the ash has a small volume and is readily disposed of The method is further economically viable because at the front end it benefits from the willingness of treatment plant operators to pay a tipping fee in order to dispose of the difficult-to-handle sewage sludge, and further because, at the other end of the cycle, the sludge will have been converted into a fuel with a positive heating value that can be used to generate further revenue or other items of value in the form of payments for the generated heat energy or, for example, trading the extracted heat for credits, desired products and the like.

Additional embodiments of the present invention will be apparent from the description and the drawings of this application.


Further features and advantages of the invention can be ascertained from the following detailed description that is provided in connection with the drawing(s) described below:

FIG. 1 is a schematic flow diagram illustrating the process of the present invention for converting biosolids into a high energy density slurry or dry solid fuel as a renewable energy source;

FIG. 1A is a schematic flow diagram similar to FIG. 1 illustrating another process of the present invention for converting biosolids into a high energy density slurry or dry solid fuel as a renewable energy source;

FIG. 2 is a flow diagram in which the process of the present invention is used in a wastewater treatment plant;

FIG. 3 is a flow diagram in which the process of the present invention is used in the operation of a cement kiln;

FIG. 4 is a flow diagram in which the process of the present invention is employed in the operation of a thermal power station using additional fuels, such as low-rank coals; and

FIG. 5 is a flow diagram in which the process of the present invention is combined with a thermal dryer and used in a cement kiln.


FIG. 1 illustrates the conversion of biosolids to a viable renewable fuel. Biosolids may be delivered as sludge via a pipeline 107 from an adjacent wastewater or sewage treatment plant (WWTP) to a raw feed tank 106. Alternatively, biosolids may be delivered by a truck 108 and pumped by a sludge pump 109 via a line 110 to the tank 106.

Alternatively, the raw feed tank 106 can receive biosolids from multiple sources and be utilized as a mixing vessel whereby more dilute biosolids are mixed with thicker, more viscous biosolids to render a more pumpable feed. A commingling and slurrying facility 104 can also be utilized for this purpose.

In addition, the raw feed tank 106 or comminuting commingling and slurrying facility 104 can be the points whereby polymer is added to reduce the water content of the biosolids slurry or, alternatively, where water is added if the viscosity of the slurry is an issue.

Heat may be added to the tank 106 to enhance the viscosity of the biosolids. In addition, a shearing or grinding step may be added, for instance between the raw feed tank 106 and a pumping device 111. This shearing or grinding will lower viscosity as well as achieve the particle size uniformity necessary for optimal operation of a pressure let-down valve 116. Addition of heat, shearing and grinding will also enhance the performance of the pumping device 111 and allow a higher solids content material into the system.

In one embodiment, a screening device is added to remove large particle-size items to enhance the performance of any grinding, the pumping device 111 and/or the pressure let-down valve 116. For example, the screening device may be placed between the raw feed tank 106 and the pumping device 111. In another embodiment, the raw feed tank 106 or a similar device can be used to add a chelating agent or other suitable chemical to remove phosphorus or other elements found in the biosolids.

From the raw feed tank 106, the biosolids slurry is pumped to a pressure that will keep the water in the slurry in liquid phase during subsequent heating operations. For example, in one embodiment, the slurry is at a pressure ranging from about 400 to 1200 psi. In another embodiment, the pressure of the slurry is between about 250 to 1600 psi. Care must be exercised to provide a pumping device 111 with an adequate net pump suction head (NPSH), either hydraulically or by mechanical assistance, as with a screw conveyor, considering that the slurry may be very viscous and may carry dissolved gases.

An alternative (not shown), for reducing the service of the pumping device 111, is the addition of booster pumps in the process anywhere between the pumping device 111 and the let-down valve 116. A further alternative (not shown) for reducing the service of the pumping device 111 is the addition of freed water or reacted slurry before the pumping device 111.

The biosolids slurry is pumped through heat exchangers 112 and 113 before passing to a reactor 114. While passing through the heat exchanger 112 the slurry is heated by exchange with hot liquid heat transfer fluid (HTF), such as Therminol 59. In another embodiment (not shown), the slurry may be heated via heat exchange with steam, either directly or indirectly. The outlet temperature of the slurry leaving heat exchanger 112 may range from about 150° C. to 315° C. (300° F. to 600° F.), and is preferably between about 200° C. to 260° C. (400° F. to 500° F.). While passing through the heat exchanger 113, the slurry is further heated to the desired temperature at which the biosolids cell walls will rupture and to liberate water bound in the cells. The temperature is further preferably set so that the other constituents of the biosolids cells are carbonized to convert these constituents to char by heat exchange with hot liquid HTF. In an alternate embodiment, the condensing vapor of a vaporizable HTF, such as Therminol VP-1, is used to heat the slurry to the desired temperature. In one embodiment, this temperature is between about 200° C. to 260° C. (400° F. to 500° F.). In another embodiment, the temperature is between about 150° C. to 260° C. (300° F. to 500° F.). In still another embodiment, the temperature is between about 260° C. to 350° C. (500° F. to 650° F.).

While the design of the heat exchangers for use with the present invention is not critical, each may comprise two or more shells. The shells may be in parallel or in series. In one embodiment, the heat exchangers 112 and 113 are arranged in a series such that the biosolids slurry passes through heat exchanger 112 prior to heat exchanger 113.

The reactor 114 (which may comprise one or more reactors in parallel or series) provides time at elevated temperature to first rupture the biosolids cells and further to complete the deoxidation reactions to convert the cell constituents to char. While a continuous reaction is discussed here, the present invention also contemplates a batch or semi-batch reaction. As known to those of ordinary skill in the art, the methods for heating the batch reactors can be similar to those for a continuous reactor. For example, a batch reactor may be heated by direct steam injection, heating coils, or a combination thereof.

One suitable alternative (not shown) for reactor 114 is a reactor-stripper tower. Such a tower has side-to-side baffles (or other vapor-liquid contacting media) arranged for downflow of partially heated slurry from the exchanger 112 contacting an upflow of steam and stripped carbon dioxide from a “reboiler” (the equivalent of exchanger 113), receiving char slurry from the base of the tower. The tower preferably has a top-to-bottom temperature gradient from approximately the slurry outlet temperature of the exchanger 112 to a temperature somewhat lower than that leaving the illustrated simple reactor. In one embodiment, the temperature gradient ranges from about 200° C. to 260° C. (400° F. to 500° F.). In another embodiment, the temperature gradient is between about 150° C. to 315° C. (300° F. to 600° F.). The carbon dioxide leaving the top of the reactor-stripper contains appreciable water vapor that needs to be condensed in a new condenser to distilled water and separated from carbon dioxide which leaves via a line 118. While the let-down valve 116 and separator 117 are still required, little carbon dioxide remains to be separated in the separator.

The slurry leaving the reactor (or reactors), referred to as char slurry, consists of destroyed biosolids cells from which the bound water has been freed and which has also undergone fluid deoxidation, i.e. a molecular rearrangement characterized by splitting off carbon dioxide, resulting in a substantial increase in solids carbon content and a substantial decrease in solids oxygen content. For example, char samples are comprised of about a 2% to 15% increase in solids carbon content, preferably with about a 4% to 12% increase. In one embodiment, the solids oxygen content decreases by about 35% to 50%. In another embodiment, the slurry undergoes a decrease in solids oxygen content of about 30% to 70%.

Char slurry flows from the reactor 114 to the heat exchanger 115, where it is partially cooled by giving up heat to the liquid HTF which comes to it from the exchanger 112 via a line 142. In one embodiment, the char slurry is cooled to a temperature ranging from about 150° C. to 200° C. (300° F. to 400° F.). In another embodiment, the temperature of the char slurry after leaving heat exchanger 115 is between about 100° C. to 260° C. (200° F. to 500° F.). The liquid HTF circuit is completed by a liquid HTF receiver 139, a liquid HTF pump 140 and connecting lines 141, 142 and 143.

The services of the heat exchangers 112 and 115 (FIG. 1) could be performed by a single exchanger 160 (FIG. 1A) having the cold feed slurry on one side and the hot char slurry on the other, which would require passing slurries through both the tube and the shell sides. Any deposits on the tube side of the heat transfer service would be relatively easy to clean. Fouling on the shell side would be difficult to correct, however, and heat transfer coefficients are much lower with a product-to-product exchanger. As such, the present invention contemplates dividing the service into two exchangers, with clean HTF being a “go-between”, both hot and cold slurries then being on the tube sides, with only clean HTF on the shell sides. The duties of the two exchangers are essentially the same (differing only by radiation loss), the temperature ranges of the circulating HTF seeking their own equilibrium.

In one embodiment, reacted biosolids char leaving the reactor 114, while still under pressure, is recycled via recycle line 162 back to the pressurized biosolids slurry before it enters the reactor 114, as shown in FIG. 1A, in order to facilitate heating and reduce the viscosity of the slurry prior to biosolids cell destruction and subsequent deoxidation.

Vaporized HTF flows from a receiver 144, through a line 145, to the hot side of the exchanger 113, in which it is condensed by the transfer of heat to partially heat the biosolids slurry, and then flows by means of a line 146 back to the receiver 144. Liquid HTF flows from the receiver 144 by natural convection (or a furnace charge pump, not shown, if pressure drop requires this) through the coils of a fired heater 147, where it is partially vaporized by heat supplied by a fuel source 148 and flows back to the receiver 144. In one embodiment, the fuel source is natural gas, propane, fuel oil, char slurry, char, or any combination thereof. In an alternate embodiment (not shown), a combustion device, such as a fluid bed, is employed to use char, char slurry, or a combination of char and an outside fuel source or waste source. In another embodiment (not shown), a gasifier is employed to use char, char slurry, or a combination of char and an outside fuel source or waste source. In yet another embodiment, a boiler is used to generate steam for process heat. The boiler could use char, char slurry, or a combination of char and an outside fuel source or waste source.

An HTF pump 149 takes suction from the bottom of the receiver 144 and circulates liquid vaporizable HTF to a facility 135 as a source of heat for char drying. After serving this purpose, it is returned, via line 150, to the receiver 144. The pump 149 may also serve other auxiliary heating services (not shown) such as to a jacket for the reactor 114 to prevent heat loss.

After being partially cooled in the heat exchanger 115, the now-fluid char slurry flows through a cooler 119, in which its temperature is lowered to near ambient by exchange with plant cooling water from a line 120. The cooled char slurry flows from cooler 119 to an automatic pressure let-down valve 116, which has been responsible for maintaining the aqueous slurries under sufficient pressure to avoid vaporization. The pressure let-down valve 116 reduces the pressure of the char slurry to a nominal pressure above atmospheric. This is achieved by liberating gaseous and dissolved carbon dioxide, which is separated from the char slurry in a separator drum 117. Evolved carbon dioxide exits the separator drum 117 via aline 118.

The pressure let-down valve 116 is subjected to strenuous conditions and has a high potential for clogging. Certain steps can be performed, however, to minimize these difficult conditions. For example, as previously mentioned, grinding or screening can be performed anytime before the pressure let-down valve 116. In addition, a step prior to the pressure let-down valve 116 of further cooling the reacted slurry after the heat exchanger 115, as shown, will reduce the amount of evolved gas and reduce the acceleration of particles across the pressure let-down valve 116. Those of ordinary skill in the art will appreciate that several cooling techniques are suitable for use with the present invention. Cooling techniques could include counter-current shell and tube or double-pipe exchanger cooled by plant cooling water.

Because foaming may occur in either the storage tank 121 or the drum 117, it may be advantageous to control foaming by letting down pressure in two or more stages. In another embodiment, foaming may be controlled by using a spray nozzle from the lower part of the drum 117 to spray a side stream into the drum 117.

Some dissolved carbon dioxide separates in the tank 121 and leaves via a line 137. If there is a use or market for carbon dioxide, this gas, along with that evolved in the drum 117, leaving via the line 118, may be subjected to purification. Otherwise, it will be collected and discharged through the flame of a fired heater 147 to destroy traces of odor-causing gases and/or for energy recovery. Approximately 25 to 27 pounds of carbon dioxide are released per ton of wet biosolids processed. Any sulfur compounds in the carbon dioxide will be treated with the necessary pollution control devices. All vent gases are conducted to the fired heater 147 to destroy traces of odor-causing gases.

Liquid char slurry flows from the bottom of the tank 121 to a dewatering facility 122, where one or more commercially-available devices for the mechanical separation of liquids and solids is employed to separate the freed water from the char solids. Suitable separation devices may include, but are not limited to, thickeners, hydroclones, centrifuges, pressure and vacuum rotary filters, horizontal filters, belt and rotary presses, and the like.

Liquid char slurry in the tank 121 will contain some heat and may be ideal for a further step of adding a chelating agent or other chemicals to remove phosphorus or other elements found in the original biosolids. The chelating agents discussed above are also suitable for use at this stage in the process.

Char solids leave the dewatering facility 122 via a conveyance means 123. Some or all of them may be directed to an eductor 124 in which they are mixed with sufficient water from a line 125 to form a pumpable, high energy density fuel slurry. The fuel slurry is accumulated in a tank 126 for off-loading to a pipeline or tank truck, as required, by means of a fuel slurry pump 151 and a line 152. Alternatively, the damp char may be conveyed by conveyance means 127 and 128 to a damp char hopper 136 to be off-loaded, as required, into hopper-bottom trucks 156.

Alternatively, part or all of the char leaving the dewatering facility 122 can be directed to a drying and/or pelletizing facility 135 via conveyance means 127, which, utilizing commercially-available equipment, dries and compacts or pelletizes the solids. Heat required for the drying is supplied by a stream of hot liquid HTF from a vaporizable HTF receiver 144 by a HTF pump 149 which, after providing the necessary heat, is returned, via line 150, to the receiver. Dried char fuel is accumulated in a dried char silo 153, to be off-loaded to hopper-bottom trucks 155 and transported to market. In one embodiment (not shown), dried char fuel is cooled prior to being accumulated in the dried char silo 153. In another embodiment, the dried product is stored under nitrogen blanket to prevent dust explosions and fire in the event that the product is not transported directly from the facility. Evaporated water from the dryer 135 flows through a condenser 138, and the condensate is transported via a line to the freed water tank.

In one embodiment (not shown), the heat required for the drying facility 135 can be produced by at least one of the methods of a fluid bed, boiler, or combusting gas from a gasifier. The fuel source for the heat required for the drying could be at least one of char, char slurry, or a combination of char and an outside fuel source or waste source. In one embodiment (not shown), the gas from a digester at an adjacent wastewater treatment plant is utilized as fuel for at least one of the process heater and the dryer.

Although not shown in FIG. 1, nor entirely renewable, char dried in the drying facility 135, but not pelletized, may be diverted to a mixing device with which it is incorporated into a fuel oil. The technology resembles that of the coal-oil mixture (COM) programs developed and tested in the 1980s. While not conforming to existing fuel oil specifications, such an addition would add heating value and, in some cases, reduce the sulfur content at low cost. This new fuel is of interest for users where ash is not a problem, such as in cement kilns and blast furnaces. Although any grade of distillate or residual fuel oil can be used, most likely candidates are off-spec slop oils, refinery fuel, used lube oil, and the like. The oil-char slurry is also attractive for in-plant fuel uses.

Freed water separated from damp char in the facility 122 flows through a line 129 to a freed water tank 130, from which it is pumped by a freed water pump 131, either via a line 132 to a comminuting and slurrying facility 104 and/or tank 106, and/or it is returned to the wastewater treatment plant (WWTP) via line a 134. Depending on the rate scale for treatment at the WWTP, it may be economical to employ some pretreatment, by known commercial means, in a pretreatment facility 133. Any sludge which is derived from the pretreatment facility can be conveyed to the drying facility 135. As discussed earlier, the dried product may be stored under nitrogen blanket or other method to prevent dust explosions.

While the process flow diagram of FIG. 1 has been described with respect to the treatment of large amounts of biosolids, as accumulate most frequently at municipal sewage and wastewater treatment plants, those of ordinary skill in the art will appreciate that other substances, such as biomass, can be dewatered with the general process of the invention in addition to the biosolids to enhance the amount of fuel being generated. For example, fluid biomass wastes, such as papermill and paper recycling sludges, may be charged via a tank truck 108 or a pipeline 107 or a pump 109 and line 110. If the waste contains appreciable amounts of chlorine compounds, alkali of at least the chemical equivalent of the chlorine is also added (not shown). Solid biomass wastes, as from agriculture and forestry, may be charged via a conveyor 101 to the comminuting and slurrying facility 104, employing known technology described, for example, in U.S. Pat. No. 5,685,153, the entire disclosure of which is incorporated by reference herein. Low-grade carbonaceous fuels, such as Powder River Basin sub-bituminous coal, may alternatively or additionally be charged to the facility 104 via a conveyance means 102. Recycled water is added to the facility as required for specified slurry viscosity by means of the line 132, and/or fresh water by means of the line 103. As outlined above with respect to the biosolids, the slurried hydrophilic feedstock is transferred via a line 105 to the storage tank 106.

The high reactivity of the biosolids char, as produced by a unit exemplified by FIG. 1, has been noted. This property of its carbonaceous molecules will be useful to a gasification facility, or a chemical plant using it as raw material for oxygenated organic compounds, either low molecular weight (such as acetic acid, alcohols, aldehydes and ketones) or higher molecular weight detergents, surfactants, plasticizers, lubricating oil additives, and the like. Among the future possibilities for char gasification is the shifting of the CO content of the gas to carbon dioxide and hydrogen, with subsequent separation of the carbon dioxide to yield hydrogen for fuel cells. This separation may well be performed by the new metal-ceramic membranes being developed for the U.S. Department of Energy (DOE) FutureGen project, in collaboration with Oak Ridge National Laboratory and Eltron Research.

FIG. 2 is a flow diagram of a combination of a wastewater treatment plant (WWTP) operating in accordance with the present invention and, adjacent thereto, an efficient biosolids processing facility operating in accordance with the present invention and employing fluid deoxidation to economically convert biosolids into a combustible material, resulting in the elimination of most of the water from WWTP biosolids, and particularly the water bound in the biosolids cells, that otherwise inflate the cost of transporting and/or evaporating the water from the biosolids and thereby make the use of biosolids unfeasible. Combustible gas from the WWTP's anaerobic digestion may be used to provide heat needed for the deoxidation, thus saving the cost of purchased fuel. Furthermore, treated water from the WWTP can be utilized for slurrying water for the fluid deoxidation unit. Moreover, the WWTP can also treat the effluent from the deoxidation unit.

In particular, WWTP 201 receives storm drainage via one or more conduits 203 and sewage via one or more conduits 204. Using known technology, a WWTP typically employs atmospheric air entering via a conduit 205 and various customary additives, such as flocculants and lime, via a transport system 206. This conventional treatment of sewage and wastewater results in the production of a digester gas, leaving the WWTP via a conduit 207, which is utilized as a fuel source for the present invention. The treatment produces a viscous sewage sludge, i.e. a sludge or slurry of biosolids leaving through a line 208. The concentration of solids will typically be in the range of between about 3% to 40% and averaging about 20%. Because biosolids contain about 80% bound water, they are expensive to haul to acceptable disposal sites, to combust with the water present, or to attempt to physically dewater them.

A deoxidation unit 202, employing the process of FIG. 1, is installed as close as feasible to the source of the biosolids. By rupturing the cellular structure and splitting off carbon dioxide from the molecules making up the biosolids, the slurry is readily mechanically dewatered to contain about 35% to 65% solids. The now-separable (freed) water (about 90% of that in the raw biosolids) is recycled to the WWTP through a line 211, where it may be pretreated with membranes, ammonia removal technologies, anaerobic digestion technologies, or reverse osmosis technologies. Upon drying, the char remaining has only about 15% to 17% of the weight of the raw biosolids, resulting in large cost savings for transporting the char to a point of use or disposal.

Undried low-moisture char, exiting via suitable means 210, may be acceptable at a nearby landfill, to which it is transported by a suitable conveyor or carrier 212. It may similarly be transported to a nearby incinerator, via a means 213, where its incineration will require much less fuel than the corresponding raw biosolids would consume. In addition, either dried or undried char may be transported to a nearby cement kiln, via a means 214, where it requires significantly less purchased fuel than would be needed for an equivalent amount of raw biosolids. The char may also be transported, via a means 215, to a chemical plant where (aided by high reactivity) it is readily converted to fuel or synthesized gas, to oxygenated compounds, to carbon fibers, to fertilizer production, and/or to landfill. The low-moisture char may be transported, by a means 216, either as a pumpable slurry or as dry pellets, to a thermal power station where its high reactivity permits efficient combustion with low excess air and high carbon burnout.

Equally as significant as the flow of materials and energy is a flow of money, in the form of a tipping fee, from the WWTP to the biosolids processing unit, as indicated by a dashed line 217. The tipping fee is the fee paid by the WWTP to the owner of the processing unit for managing its biosolids.

Since the supply of the new fuel discussed above will initially be small, it is optimal for local use. As such, one of the first fuel users to accept it is likely to be cement kiln operators, since they can to a large extent tolerate its high ash content. Other suitable areas of use are blast furnaces and foundries, since they are accustomed to firing coal or coke and to disposing of ash with other impurities as slag. As the supply of biosolids char increases, it will become of interest to general coal users, including thermal power stations. Such applications are addressed in more detail in the remaining figures.

For example, FIG. 3 is a flow diagram illustrating an efficient biosolids processing facility for converting biosolids into a combustible, preferably carbonized material that is combined with a cement kiln. This aspect of the present invention highlights the drastic reduction of water that would otherwise accompany raw biosolids into the kiln, enabling a substantial increase in the amount of biosolids consumed, with a proportionate increase in tipping revenue received by the processor and Btus charged to the kiln.

In particular, a fluid deoxidation unit 301, employing the process described with respect to FIG. 1, is installed as close as feasible to one or more WWTPs, the source of the biosolids, as indicated by a transport means 303. By rupturing the biosolids cell walls and discharging carbon dioxide that may be formed at the same time (line 304), the resulting char can now be readily mechanically dewatered to comprise about 35% to 65% solids. The now-separable water (about 90% of that in the raw biosolids) is recycled to the WWTP through a line 305 or is used as recycle water for process slurrying.

Char, either as a concentrated slurry, a wet solid, or a dried solid, is transported to a cement kiln 302 via a transport means 306. The basic ingredients of Portland cement (limestone, clay and shale) are charged via conduits 307, 308 and 309, and are ground, mixed and charged to the kiln through a conduit 310. In a preheat section, these ingredients are contacted counter-currently with hot flue gas, which raises the temperature to drive off water of crystallization and calcine the limestone. Near the bottom of the preheat section, waste combustibles, such as used tires and broken asphalt, are charged through a conduit 311. If necessary to achieve the desired temperature, fuel such as coal, oil or gas is fired, together with combustion air, into the lower part of the preheat section. The preheated mix is then discharged into one end of a horizontal, rotating kiln.

As the preheated ingredients travel to the opposite end of the rotating kiln, they are further heated to the temperature necessary for them to react and form cement clinker by firing, at a discharge end, primary fuel delivered through a conduit 312 (which may include biosolids char), along with the corresponding combustion air supplied via a combustion air fan (not shown) and a conduit 313.

Flue gas, from which most of the sensible heat has been recovered, leaves the kiln via an exhaust fan and dust recovery equipment (not shown) through a line 314. Cement clinker exits the kiln via heat exchange with combustion air, through a conduit 315. The cooled clinker is ground and blended with gypsum to form Portland cement.

Most of the ash constituents of biosolids char are tolerable in Portland cement, with the exception of soluble cations, such as sodium and potassium and the sulfates and chlorides, which go primarily to the effluent from the liquid deoxidation unit and are returned via a conduit 305 to the WWTP. The exception is phosphorus, which often is bound in insoluble form by iron. It is possible that the phosphorus content could limit the amount of biosolids char a given cement kiln can accept. Should the content of phosphorus in the char produced by the unit 301 be so high as to limit the amount of biosolids char that can be accepted in the cement clinker, a chelate solution (or other solublizing agent) may be employed via a line 316 to extract some of this element. The phosphorus-containing extract is then discharged through a line 317 and must be disposed of in a manner that avoids returning it to the WWTP.

The inorganic fraction of biosolids can be as high as about 50% on a dry basis. This inherent ash found in biosolids can reduce the quantities of limestone, clay and shale input in lines 307, 308 and 309, respectively. If unit 301 is located near the cement kiln 302, a portion of a wastewater stream 305 can be utilized in the cement kiln 302 for cooling or other purposes, or in NOx reduction. Waste heat from the stream 314, or other waste heat streams, including radiation heat, can be utilized by unit 301 as process heat for the system including heating the feed material, process heat, or drying the reacted product. Evolved carbon dioxide from the stream 302 can be conducted to the cement kiln 302 for heat recovery or odor reduction.

Equally as significant as the flow of materials and energy is a flow of money, in the form of tipping fees, from the WWTP to the combination of units 301 and 302, as indicated by the dashed line 318. A portion of the fee goes to the owner of the unit 301, as indicated by a dashed line 319, and the remainder goes to the owner of the cement kiln 302 as indicated by a dashed line 320.

FIG. 4 is a simplified flow diagram of an efficient biosolids processing facility 401 employing deoxidation to convert biosolids into a combustible material in close proximity to and combined with a thermal power station 402. The unit 401 is typified by FIG. 1, charging biosolids from a WWTP. However, since the supply of biosolids available to a station of economic size is unlikely to be sufficient for its fuel needs, it also represents a family of liquid deoxidation processes charging a spectrum of renewable biomass and/or hydrophilic low-rank fossil fuel. With any or all of these potential fuels, liquid deoxidation makes them less hydrophilic and more uniform and thermally efficient for combustion in the power station 402. The station 402 represents a spectrum of conventional and unconventional combustion systems culminating, via steam turbine or gas turbine combined cycles, in the production of electricity for the local market and/or the national grid.

Biosolids are charged to the unit 401 via a line 403. Alternatively or additionally, biomass waste, as paper mill sludge or from agriculture or forestry, is delivered by a transport means 404, and (optionally) hydrophilic low-rank fossil fuel is delivered through a transport means 405. Water as required to form a pumpable charge slurry is added through a line 406. After being processed according to FIG. 1, the now excess water is returned to a WWTP, or treated for discharge by known means, via a line 407. Uniform (dewatered) high energy density char slurry, or dried and pelletized char, is delivered through a transport means 408 to the station 402.

The char or char slurry transported by the transport means 408 is combusted by one of the known methods to yield thermal energy for the generation of steam, which is expanded through conventional steam turbines driving electric generators, or it may be partially oxidized (with either air or commercial oxygen) to yield a fuel gas subsequently burned in a gas turbine combustor driving an electricity generator, the hot exhaust gas from which generates steam for an integrated steam turbine-driven generator. The partial combustion of char may be accomplished according to known processes separating the ash as a fluid slag, or in accordance with U.S. Pat. No. 5,485,728, the entire disclosure of which is incorporated by reference herein, which teaches separation of the ash particles in an aqueous slurry.

Since the amount of char available may have insufficient fuel energy to generate the amount of electricity for which there is a market, supplemental fossil fuel can be supplied via a transport means 410. Air for the combustion or partial combustion of the biomass and/or fossil fuel char is supplied through a line 411. After subjecting it to appropriate known pollution control measures, flue gas (or gases) from the combustion at the station 402 is (are) discharged through a stack 412.

Treated boiler feed water makeup is supplied through a line 413, and blowdown required to maintain boiler water within specifications is discharged via a line 414 to the unit 401, where it may comprise some of the water needed to form a sufficiently fluid feed slurry to the deoxidation operation. Ash, the non-combustible residue from burning the char and auxiliary fuels, or ash slurry, is withdrawn for disposal via a conduit 415.

One of the known methods of controlling the emission of nitrogen oxides from atmospheric pressure boilers is overfiring with a reactive fuel above the main flame zone. Because of its volatiles content and high reactivity, biosolids char is a suitable fuel for this purpose, and a portion of that from the conveying means 408 can be diverted by way of a transport means 416 for nitrogen oxide reduction. The product of the combination, electricity, is delivered from the site via electric cables 417.

For simplification, the biosolids treatment unit 401 is shown as though it had the capacity and raw material supply to furnish the power station 402 with sufficient char fuel. In a practical installation, a treatment unit 401 may be located adjacent to the power station 402, and one or more such units 401 may be installed at other location(s) close to the raw material sources. This gives the operator the flexibility to employ tailored deoxidation temperatures, optimized for the particular feedstock. In such an event, dry char can then be shipped to the power station 402 by road or rail or, if economics dictate, it can be supplied as an aqueous slurry via a pipeline. The flow of money, in the form of a tipping fee, from the WWTP to the deoxidation unit, is indicated by a dashed line 418

FIG. 5 is a simplified flow diagram of a combination comprising a thermal dryer unit 501 and a cement kiln 502. The thermal dryer unit 501 is installed as close as feasible to one or more cement kilns 502, employing principally the same configuration as shown in and described in conjunction with FIG. 3, but without deoxidizing the biosolids. Biosolids are supplied via a transport means 503. By applying heat to the raw biosolids cells, water contained in the cells is evaporated and leaves via a line 505 for scrubbing and condensing or, alternatively, is conducted via a line 517 back to the kiln to be utilized in the kiln as make-up water or for NOx reduction.

The resulting dried biosolids are conducted to the kiln via a line 506 where the Btu value as well as the value of the ash are utilized. The primary ingredients, such as are shown in FIG. 3, are added to the kiln at the lines 507, 508, 509 through a conduit 510. As in FIG. 3, in a preheat section, waste combustibles are added, such as used tires and broken asphalt charged through a conduit 511. As in FIG. 3, combustion air and primary fuel arrive via conduits 513 and 512, respectively. Cement klinker exits the kiln via a conduit 515.

Although thermal drying has an inherent energy penalty from the latent heat in the evaporation of water, this penalty can be entirely or partially overcome by integrating with the cement kiln and utilizing heat from the kiln via a conduit 518. More specifically, flue gas, normally traveling via a conduit 514 to an appropriate discharge, can be directed via a conduit 516 to the thermal dryer, thereby reducing the need for primary fuels at thermal dryer 501 for evaporating the water liberated from the biosolids.

As discussed briefly above, because the potential supply of biosolids char is smaller, by orders of magnitude, than the general fuels market, other substances, for example biomass, can be co-processed in a liquid deoxidation unit, or processed in parallel equipment, and the resulting chars blended before being used as a fuel, for example in accordance with the teachings of U.S. Pat. No. 5,485,728. Several locations, such as Hawaii (biosolids, pineapple and sugar cane wastes) and Sacramento, Calif. (biosolids and rice hulls and stalks), offer sites for slurry co- or parallel deoxidation. Paper mill and paper recycling sludges, although they may require alkali addition to neutralize chlorine, are other promising sources of supplemental hydrophilic biomass. These methods afford a means of consolidating diverse sources into a uniform liquid or solid char slurry fuel.


The following examples are only representative of the methods and systems for use in practicing the present invention, and are not to be construed as limiting the scope of the invention in any way.

Example 1

Biosolids from two wastewater treatment plants, one in Atlanta, Ga., and one in Riverside, Calif., were subjected to the earlier described treatment in a continuous pilot plant, resulting in the following feed and product analyses, reported on a moisture and ash-free basis:

Atlanta Raw Riverside Raw
Biosolids Biosolids
Carbon 57.73 62.53
Hydrogen 7.74 9.26
Nitrogen 7.90 7.52
Sulfur 3.02 1.17
Oxygen 23.86 19.52
Total 100.00 100.00

Atlanta Char Riverside Char
Product Product
Carbon 70.19 69.98
Hydrogen 8.85 7.68
Nitrogen 8.63 8.45
Sulfur 1.42 8.86
Oxygen 10.91 5.04
Total 100.00 100.00

As would be expected, the splitting off of carbon dioxide has resulted in an increase in carbon content and a corresponding decrease in oxygen content.

The off-gas composition of the two runs was as follows:

Atlanta Riverside
Off Gas Off Gas
Carbon dioxide 89.7% 92.8%
Volatile organics 10.0% 6.0%
Sulfur compounds 0.3% 1.2%
Total 100.0% 100.0%

Theoretical Example 1

A cement kiln in the southwestern U.S. has a production capacity of 3,200 tons/day. To reach temperatures required to form cement “clinker”, it fires low-grade coal, supplemented to some extent by charging scrap rubber tires. Sensible heat in the flue gas, after preheating mineral charge and combustion air, may be taken advantage of to dry and incinerate 20 tons/day (dry basis) of biosolids from area wastewater treatment plants. Although every ton of dry biosolids constituents is accompanied by about four tons of water (giving the biosolids a negative heating value), revenue from the tipping fee offsets the cost of extra coal that must be fired. However, the amount is limited by the thermal capacity to evaporate the water and by the increased volume of flue gas, increasing pressure drop and fan horsepower.

Using this invention, the kiln may use biosolids dewatered and deoxidized in accordance with the present invention at one or more of the nearby WWTPs. As such, about 80% to 94% of the water formerly charged with the raw biosolids bypasses the kiln, permitting it to charge seven times as much deoxidized material without exceeding thermal capacity and fan horsepower limits. The biosolids disposed of by the kiln can be increased by a factor of about 700%, with a corresponding increase in tipping fees.

Other than in the operating examples, or unless otherwise expressly specified, all of the numerical ranges, amounts, values and percentages such as those for amounts of materials, times and temperatures of reaction, ratios of amounts, and others in the following portion of the specification may be read as if prefaced by the word “about” even though the term “about” may not expressly appear with the value, amount or range. Accordingly, unless indicated to the contrary, the numerical parameters set forth in the following specification and attached claims are approximations that may vary depending upon the desired properties sought to be obtained by the present invention.

Notwithstanding that the numerical ranges and parameters setting forth the broad scope of the invention are approximations, the numerical values set forth in the specific examples are reported as precisely as possible. Any numerical value, however, inherently contains certain errors necessarily resulting from the standard deviation found in their respective testing measurements. Furthermore, when numerical ranges of varying scope are set forth herein, it is contemplated that any combination of these values inclusive of the recited values may be used.

The invention described and claimed herein is not to be limited in scope by the specific embodiments herein disclosed, since these embodiments are intended as illustrations of several aspects of the invention. Any equivalent embodiments are intended to be within the scope of this invention. Indeed, various modifications of the invention in addition to those shown and described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are also intended to fall within the scope of the appended claims. All patents and patent applications cited in the foregoing text are expressly incorporated herein by reference in their entirety.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US35801935 Sep 196925 May 1971Dorr Oliver IncHeat treated waste sludge disposal
US372904222 Feb 197124 Apr 1973Pollutant Separation IncApparatus for separating pollutants and obtaining separate liquids & solids
US383063630 Nov 197120 Aug 1974Black Clawson Fibreclaim IncFuel by-products of municipal refuse
US385375919 Nov 197010 Dec 1974J TitmasDynamic hydraulic column activation method
US401742116 Dec 197512 Apr 1977Othmer Donald FWet combustion process
US403815211 Apr 197526 Jul 1977Wallace-Atkins Oil CorporationProcess and apparatus for the destructive distillation of waste material
US408727615 Jul 19772 May 1978Anic S.P.A.Removal of mercury from sludge by heating and condensing
US412651912 Sep 197721 Nov 1978Edward KoppelmanApparatus and method for thermal treatment of organic carbonaceous material
US41289468 Mar 197712 Dec 1978Uop Inc.Organic waste drying process
US419265329 Dec 197711 Mar 1980Gulf Research And Development CompanyNovel fuel compositions comprising upgraded solid _and/or semi-solid material prepared from coal
US42082457 Sep 197817 Jun 1980St. Regis Paper CompanyPyrolysis of spent pulping liquors
US42292963 Aug 197821 Oct 1980Whirlpool CorporationWet oxidation system employing phase separating reactor
US42417222 Oct 197830 Dec 1980Dickinson Norman LPollutant-free low temperature combustion process having carbonaceous fuel suspended in alkaline aqueous solution
US425512911 Jul 197910 Mar 1981Thomas N. DePewApparatus and method for processing organic materials into more useful states
US42723223 Apr 19799 Jun 1981Masahiro KobayashiMethod for manufacturing charcoals from paper sludge
US428401526 Mar 197918 Aug 1981Dickinson Norman LPollution-free coal combustion process
US42929535 Oct 19786 Oct 1981Dickinson Norman LPollutant-free low temperature slurry combustion process utilizing the super-critical state
US437706627 May 198022 Mar 1983Dickinson Norman LPollution-free pressurized fluidized bed combustion utilizing a high concentration of water vapor
US43809606 May 198126 Apr 1983Dickinson Norman LPollution-free low temperature slurry combustion process utilizing the super-critical state
US441481324 Jun 198115 Nov 1983Knapp Hans JPower generator system
US447725713 Dec 198216 Oct 1984K-Fuel/Koppelman Patent Licensing TrustApparatus and process for thermal treatment of organic carbonaceous materials
US448695927 Dec 198311 Dec 1984The Halcon Sd Group, Inc.Process for the thermal dewatering of young coals
US457956216 May 19841 Apr 1986Institute Of Gas TechnologyThermochemical beneficiation of low rank coals
US459320225 Apr 19833 Jun 1986Dipac AssociatesCombination of supercritical wet combustion and compressed air energy storage
US461571116 Aug 19857 Oct 1986Mueller DietrichSewage sludge fuel briquette
US461873529 Aug 198421 Oct 1986Canadian Patents And Development LimitedProcess and apparatus for the conversion of sludges
US465768122 Apr 198514 Apr 1987Hughes William LMethod of converting organic material into useful products and disposable waste
US47027451 May 198627 Oct 1987Kawasaki Jukogyo Kabushiki KaishaProcess for dewatering high moisture, porous organic solid
US471403226 Dec 198522 Dec 1987Dipac AssociatesPollution-free pressurized combustion utilizing a controlled concentration of water vapor
US47215753 Apr 198626 Jan 1988Vertech Treatment Systems, Inc.Method and apparatus for controlled chemical reactions
US473572920 Jun 19865 Apr 1988Zimpro Inc.Ash concentration and disposal method
US476189329 Oct 19869 Aug 1988Glorioso John DSludge treatment process
US476252716 Dec 19869 Aug 1988Electric Fuels CorporationSlurry fuel comprised of a heat treated, partially dewatered sludge with a particulate solid fuel and its method of manufacture
US476591114 Sep 198723 Aug 1988North American Metals, Inc.Process for treating municipal wastewater sludge
US47955683 Jun 19873 Jan 1989Chen Philip TOxidative evaporation process and apparatus
US482456126 Jan 198825 Apr 1989Basf CorporationWastewater treatment
US48296788 Aug 198816 May 1989Enviro Gro TechnologiesSludge treatment process
US485226912 Sep 19881 Aug 1989Enviro-Gro Technologies, Inc.Combined sewage and lime slude treatment process
US486067118 Jul 198829 Aug 1989Enviro-Gro Technologies, Inc.Odor control for a sludge treatment process
US486983327 Nov 198726 Sep 1989Vertech Treatment Systems, Inc.Method and apparatus for controlled chemical reactions
US487590514 Nov 198824 Oct 1989Solidiwaste Technology, L.P.Method of preparing a high heating value fuel product
US48981079 Jan 19896 Feb 1990Dipac AssociatesPressurized wet combustion of wastes in the vapor phase
US490989921 Sep 198720 Mar 1990A. Ahlstrom CorporationMethod of concentrating sludges
US49157063 Mar 198710 Apr 1990Daley Ralph DCoal-water fuel production
US49228416 Jun 19898 May 1990Kent John MMethod and apparatus for using hazardous waste to form non-hazardous aggregate
US49534789 May 19894 Sep 1990Enviro-Gro TechnologiesOdor control for a sludge treatment process
US495692618 May 198918 Sep 1990Enviro-Gro TechnologiesSludge treatment process
US49832963 Aug 19898 Jan 1991Texaco Inc.Partial oxidation of sewage sludge
US498378227 Feb 19898 Jan 1991Veba Oel Entwicklungs-Gesellschaft MbhProcess for treating wastes and the like by low temperature carbonization and further processing of the low temperature carbonization oil
US49893444 Aug 19885 Feb 1991Enviro-Gro TechnologiesParticulate removal for a sludge treatment process
US500009929 Dec 198819 Mar 1991Dipac AssociatesCombination of fuels conversion and pressurized wet combustion
US500976721 Sep 198923 Apr 1991Mobil Oil CorporationRecycle of oily refinery wastes
US501845624 Feb 198928 May 1991Williams Patent Crusher And Pulverizer CompanySystem for disposing of sludge
US501913517 May 198828 May 1991Battelle Memorial InstituteMethod for the catalytic conversion of lignocellulosic materials
US505037521 Jul 198924 Sep 1991Dipac AssociatesPressurized wet combustion at increased temperature
US50572318 Nov 199015 Oct 1991Zimpro Passavant Environmental Systems, Inc.Method for starting up and controlling operating temperature of a wet oxidation process
US50750151 May 199124 Dec 1991Zimpro Passavant Environmental Systems, Inc.Method for color removal from thermally conditioned sludge liquors
US508257113 May 199121 Jan 1992Zimpro Passavant Environmental Systems Inc.Caustic sulfide wet oxidation process
US50873707 Dec 199011 Feb 1992Clean Harbors, Inc.Method and apparatus to detoxify aqueous based hazardous waste
US508737831 May 199011 Feb 1992Pori, International, Inc.Process for enhancing the dewaterability of waste sludge from microbiological digestion
US511454113 May 199119 May 1992Ernst BayerProcess for producing solid, liquid and gaseous fuels from organic starting material
US513200725 May 199021 Jul 1992Carbon Fuels CorporationCo-generation system for co-producing clean, coal-based fuels and electricity
US51835776 Jan 19922 Feb 1993Zimpro Passavant Environmental Systems, Inc.Process for treatment of wastewater containing inorganic ammonium salts
US51887392 Dec 199123 Feb 1993Texaco Inc.Disposal of sewage sludge
US51887402 Dec 199123 Feb 1993Texaco Inc.Process for producing pumpable fuel slurry of sewage sludge and low grade solid carbonaceous fuel
US51887411 Apr 199223 Feb 1993Texaco Inc.Treatment of sewage sludge
US520590611 Feb 199127 Apr 1993Chemical Waste Management, Inc.Process for the catalytic treatment of wastewater
US521172319 Sep 199118 May 1993Texaco Inc.Process for reacting pumpable high solids sewage sludge slurry
US521172415 Apr 199118 May 1993Texaco, Inc.Partial oxidation of sewage sludge
US52176252 Oct 19928 Jun 1993Texaco Inc.Process for disposing of sewage sludge
US522148019 Nov 199122 Jun 1993Clean Harbors, Inc.Method and apparatus to detoxify aqueous based hazardous waste
US523021115 Apr 199127 Jul 1993Texaco Inc.Partial oxidation of sewage sludge
US523081025 Sep 199127 Jul 1993Zimpro Passavant Environmental Systems, Inc.Corrosion control for wet oxidation systems
US523446828 Jun 199110 Aug 1993Texaco Inc.Process for utilizing a pumpable fuel from highly dewatered sewage sludge
US523446928 Jun 199110 Aug 1993Texaco Inc.Process for disposing of sewage sludge
US523460722 Apr 199210 Aug 1993Zimpro Passavant Environment Systems Inc.Wet oxidation system startup process
US524061911 Feb 199331 Aug 1993Zimpro Passavant Environmental Systems, Inc.Two-stage subcritical-supercritical wet oxidation
US526122520 Sep 199116 Nov 1993Dipac AssociatesPressurized wet combustion at increased temperature
US52640091 Sep 199223 Nov 1993Texaco Inc.Processing of sewage sludge for use as a fuel
US526608523 Nov 199230 Nov 1993Texaco Inc.Process for disposing of sewage sludge
US527355630 Mar 199228 Dec 1993Texaco Inc.Process for disposing of sewage sludge
US528070131 Aug 199225 Jan 1994Environmental Energy Systems, Inc.Waste treatment system and method utilizing pressurized fluid
US528841322 May 199222 Feb 1994Shell Oil CompanyTreatment of a waste sludge to produce a non-sticking fuel
US529242928 Nov 19908 Mar 1994Seaview Thermal SystemsProcess for recovery and treatment of a diverse waste stream
US5292442 *1 Oct 19928 Mar 1994Texaco Inc.Process for disposing of sewage sludge
US533749614 May 199216 Aug 1994Enviro-Gro TechnologiesSludge treatment process
US533962122 Sep 199323 Aug 1994Environmental Energy Systems, Inc.Waste treatment system and method utilizing pressurized fluid
US53499104 Aug 199327 Sep 1994F. L. Smidth & Co. A/SMethod and apparatus for incinerating waste in a cement kiln plant
US535654020 May 199118 Oct 1994Texaco Inc.Pumpable aqueous slurries of sewage sludge
US537071527 Apr 19936 Dec 1994Kortzeborn; Robert N.Waste destructor and method of converting wastes to fluid fuel
US538925915 Feb 199414 Feb 1995Zimpro Environmental Inc.Preparation treatment of volatile wastewater components
US538926412 Jul 199314 Feb 1995Zimpro Environmental Inc.Hydraulic energy dissipator for wet oxidation process
US5485728 *15 Nov 199323 Jan 1996Enertech Environmental, Inc.Efficient utilization of chlorine and moisture-containing fuels
US550004415 Oct 199319 Mar 1996Greengrove CorporationProcess for forming aggregate; and product
US558279329 Mar 199510 Dec 1996Antaeus Group, Inc.Process for treating waste material
US558651016 Mar 199424 Dec 1996Cement Industry Environment ConsortiumMethod and system for controlling pollutant emissions in combustion operations
US563085416 Sep 199420 May 1997Battelle Memorial InstituteMethod for catalytic destruction of organic materials
US564141327 Oct 199524 Jun 1997Zimpro Environmental, Inc.Removal of nitrogen from wastewaters
US56851537 Jun 199511 Nov 1997Enertech Environmental, Inc.Efficient utilization of chlorine and/or moisture-containing fuels and wastes
US570741724 Jul 199513 Jan 1998Director-General Of Agency Of Industrial Science And TechnologyProcess of treating garbage with simultaneous production of methane
US571176827 Mar 199527 Jan 1998Dynecology, Inc.Sewage sludge disposal process and product
US572480521 Aug 199510 Mar 1998University Of Massachusetts-LowellPower plant with carbon dioxide capture and zero pollutant emissions
US57979727 Apr 199725 Aug 1998Dynecology, Inc.Sewage sludge disposal process and product
US581679524 May 19966 Oct 1998Cadence Environmental Energy, Inc.Apparatus and method for providing supplemental fuel to a preheater/precalciner kiln
US588825611 Sep 199630 Mar 1999Morrison; Garrett L.Managed composition of waste-derived fuel
US588830713 Sep 199530 Mar 1999Cambi AsMethod and means for hydrolysis of organic materials
US588845329 Jan 199730 Mar 1999Riverside County Eastern Municipal Water DistrictContinuous flow pasteurization of sewage sludge
US597543913 May 19982 Nov 1999Controlled Environmental Systems CorporationMunicipal solid waste processing facility and commercial ethanol production process
US602251417 Feb 19998 Feb 2000Nkk CorporationMethod for recovering phosphorus from organic sludge
US60295886 Apr 199829 Feb 2000Minergy Corp.Closed cycle waste combustion
US603686214 Aug 199814 Mar 2000Stover; Enos L.Biochemically enchanced thermophilic treatment process
US606314717 Dec 199816 May 2000Texaco Inc.Gasification of biosludge
US60962833 Apr 19981 Aug 2000Regents Of The University Of CaliforniaIntegrated system for the destruction of organics by hydrolysis and oxidation with peroxydisulfate
US61031918 Dec 199815 Aug 2000Riverside County Eastern Municipal Water DistrictContinuous flow pasteurization of sewage sludge
US6143176 *25 Apr 19977 Nov 2000Ebara CorporationMethod of converting organic wastes to valuable resources
US614613317 May 199714 Nov 2000Heidelberger Zement AgProcess for the recycling of residues for the production of portland cement clinker
US614969416 Jun 199921 Nov 2000Northwest Missouri State UniversityProcess for using animal waste as fuel
US617618723 Dec 199623 Jan 2001Cement Industry Environmental ConsortiumSludge handling and feeding system
US619708118 Mar 19996 Mar 2001Erick SchmidtMethod for bio-refining waste organic material to produce denatured and sterile nutrient products
US625690210 Jun 199910 Jul 2001John R. FlahertyApparatus and method for desiccating and deagglomerating wet, particulate materials
US636504730 May 19982 Apr 2002Applikations-und Technikzentrum für Energieverfahrens-Umwelt-, und Strömungstechnik (ATZ-EVUS)Method and device for treating biogenic residues
US64361573 Dec 199920 Aug 2002Texaco Inc.Gasification of biosludge
US647081211 Jun 199829 Oct 2002Cemex, S.A. De C.V.Method and apparatus for recovering energy from wastes by combustion in industrial furnaces
US669254411 Apr 200117 Feb 2004Ecosystems Projects, LlcMunicipal waste briquetting system and method of filling land
US674020530 Nov 200025 May 2004The United States Of America As Represented By The Secretary Of The NavyProcessing of shipboard wastewater
US687501527 Mar 20045 Apr 2005John TiernanCement producing system incorporating a waste derived fuel suspension burner for a down draft calciner
US690560031 Oct 200214 Jun 2005Ch2M Hill, Inc.Method and apparatus for the treatment of particulate biodegradable organic waste
US69137009 Mar 20045 Jul 2005Cambi AsMethod of and arrangement for continuous hydrolysis of organic material
US696256113 Nov 20028 Nov 2005Terralog Technologies Usa, Inc.Method for biosolid disposal and methane generation
US696698914 Feb 200222 Nov 2005Otv S.A.Method and installation for the thermal hydrolysis of sludge
US697396815 Jul 200413 Dec 2005Precision Combustion, Inc.Method of natural gas production
US69787257 May 200427 Dec 2005Tecon Engineering GmbhProcess and apparatus for treating biogenic residues, particularly sludges
US71014825 Aug 20035 Sep 2006Otv S.A.Method and facility for treatment of sludge derive from biological water purification facilities
US71604425 Feb 20049 Jan 2007Industrial Technology Research InstituteApparatus for reduction of biological wasted sludge
US717937918 Nov 200320 Feb 2007Ab-Cwt, LlcApparatus for separating particulates from a suspension, and uses thereof
US71890745 Feb 200113 Mar 2007Green Island Environmental Technologies Company LimitedMethod and process for co-combustion in a waste to-energy facility
US72112297 Oct 20021 May 2007Steris Europe Inc. Suomen SivuliikeMethod and apparatus for the sterilization of biological waste
US72526916 Mar 20017 Aug 2007John PhilipsonConversion of municipal solid waste to high fuel value
US72623313 Sep 200128 Aug 2007Biofuel B.V.Process for the production of liquid fuels from biomass
US730106030 Sep 200427 Nov 2007Ab-Cwt, LlcProcess for conversion of organic, waste, or low-value materials into useful products
US731183425 Oct 200625 Dec 2007Ch2M Hill, Inc.Apparatus for the treatment of particulate biodegradable organic waste
US74343325 Oct 200414 Oct 2008Lehigh Cement CompanyMethod and apparatus for drying wet bio-solids using excess heat from a cement clinker cooler
US2004002571522 Aug 200112 Feb 2004Torben BondeConcept for slurry separation and biogas production
US200401728783 Jul 20029 Sep 2004Adam KrylowiczMethod and system of generating methane and electrical energy and thermal
US2004019298018 Nov 200330 Sep 2004Appel Brian S.Process for conversion of organic, waste, or low-value materials into useful products
US2004019298118 Nov 200330 Sep 2004Appel Brian S.Apparatus and process for converting a mixture of organic materials into hydrocarbons and carbon solids
US2005010892823 Aug 200426 May 2005Foye SparksSoil mediums and alternative fuel mediums, methods of their production and uses thereof
US2005011361129 Sep 200426 May 2005Adams Terry N.Apparatus and process for separation of organic materials from attached insoluble solids, and conversion into useful products
US2005014556918 Nov 20047 Jul 2005Ulmert Hans D.Method for treatment of sludge from waterworks and wastewater treatment plants
US2005027406614 Jun 200415 Dec 2005Morton Edward LMethod and apparatus for drying wet bio-solids using excess heat from a cement clinker cooler
US200502740685 Oct 200415 Dec 2005Morton Edward LBio-solid materials as alternate fuels in cement kiln, riser duct and calciner
US200502742937 Jun 200515 Dec 2005Lehigh Cement CompanyMethod and apparatus for drying wet bio-solids using excess heat recovered from cement manufacturing process equipment
US2006006052628 Oct 200523 Mar 2006Rupert BinningMethod and apparatus for anaerobic digestion of biomasses and generation of biogas
US2007004324626 Aug 200322 Feb 2007Trevor BridleConversion of sludges and carbonaceous materials
US2007009862529 Sep 20063 May 2007Ab-Cwt, LlcDepolymerization process of conversion of organic and non-organic waste materials into useful products
US2007028920530 May 200720 Dec 2007Foye SparksSoil mediums and alternative fuel mediums, apparatus and methods of their production and uses thereof
US2008007247822 Sep 200627 Mar 2008Barry CooperLiquefaction Process
EP0328574B113 Jul 19888 Jan 1992Fhj Process B.V.Process for the conversion and working up of a mixture of organic matter, anorganic matter and water to a nearly dry product, as well as an installation for the execution of the process and application thereof by the conversion of manure slurry
EP0377832B19 Dec 198910 Mar 1993Thyssen Still Otto Anlagentechnik GmbHProcess for the treatment of biomasses, e.g. sewage sludge, manure, etc.
EP0515117B118 May 199226 Apr 1995Texaco Development CorporationPumpable aqueous slurries of sewage sludge
EP1717209A126 Apr 20052 Nov 2006Purac AbMethod and system for treating sludge
EP1894893A1 *16 Mar 20065 Mar 2008Mitsubishi Kakoki Kaisha, LtdOrganic waste disposal facility and method of disposal
JPH11171628A Title not available
WO2002036506A12 Nov 200110 May 2002Biwater Treatment LimitedMethod and apparatus for the treatment of sludge
WO2002081379A13 Apr 200217 Oct 2002Hanwha Chemical CorporationProcess for treating waste water containing a nitrous organic components
WO2005121033A13 Jun 200522 Dec 2005Fractivator OyMethod and apparatus for manufacture of a useful product from sludge, and its use
WO2006032282A123 Sep 200530 Mar 2006Cambi Bioethanol ApsMethod for treating biomass and organic waste with the purpose of generating desired biologically based products
WO2006053020A38 Nov 200515 Feb 2007Enertech Environmental IncSlurry dewatering and conversion of biosolids to a renewable fuel
WO2006117934A1 *16 Mar 20069 Nov 2006Mitsubishi Kakoki Kaisha, Ltd.Organic waste disposal facility and method of disposal
WO2009031796A22 Sep 200812 Mar 2009Pmc Korea Co., Ltd.A device capable of removal the nitrogen, phosphorus and etc. from sludge
Non-Patent Citations
1C.F. Forster, "Preliminary Studies on the Relationship Between Sewage Sludge Viscosities and the Nature of the Surfaces of the Component Particles", Biotechnology Letters, 3(12), 707-712, 1981.
2CH2MHill and Itron, Task 2.2.1 Final Report prepared for the California Energy Commission, "Commonwealth Energy Biogas/PV Mini-Grid Renewal Resources Program, Making Renewables Part of an Affordable and Diverse Electric System in California, Contract No. 500-00-036, Process Selection Report for Wastewater Treatment Plants, Project No. 2.2 Enhanced Energy Recovery Through Optimization of Anaerobic Digestion and Microturbines", Aug. 2003.
3International Search Report and Written Opinion dated Sep. 6, 2010 in International Application No. PCT/US2010/030197.
4Kelly, Harlan G., "Emergy Processes in Biosolids Treatment, 2005", Journal of Environmental Engineering and Science, May 2006.
5Neyens, E. et al., "A review of thermal sludge pre-treatment processes to improve dewaterability", Journal of Hazardous Materials, 2003, pp. 51-67.
6Partial International Search Report for International Application No. PCT/US2010/030197, Jun. 30, 2010 (6 pages).
7Presentation-EnerTech Environmental, Inc., Introduction of the Rialto Regional Biosolids Project, Oct. 23, 2003 (10 pages).
8W.L. McCabe et al., "Unit Operations of Chemical Engineering", 5th Edition, McGraw-Hill, pp. 189-191, 1993.
9Walley, Paul, "Optimising Thermal Hydrolysis for Reliable High Digester Solids Loading and Performance", 12th European Biosolids and Organic Resources Conference, 2007.
10Weemaes, Marjoleine P.J., et al., "Evaluation of Current Wet Sludge Disintegration Techniques", Centre for Environmental Sanitation, University Ghent, Ghent, Belgium, Jun. 12, 1998.
Legal Events
22 Sep 2014ASAssignment
Effective date: 20130207